Clinical Trials Directory

Trials / Unknown

UnknownNCT04200014

Bradycardia Risk Stratification With Loop Recorder After Syncope

Bradycardia High Risk Patient Identification After Syncope With Loop Recorder an Observational Study in Nancy University Hospital

Status
Unknown
Phase
Study type
Observational
Enrollment
250 (estimated)
Sponsor
Central Hospital, Nancy, France · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

Syncope is a common symptom that may be related to a conductive disorder. If no bradycardia is authenticated, it is often necessary to implant an implantable loop recorder. In somes cases, implantable loop recorder records cardiac conductive disorders. In this study, we want to try to identify a group of patients for whom we could immediately implant a pacemaker without prior implantation of an implantable loop recorder given the high probability of implantation of a pacemaker after interrogation of the implantable loop recorder. It would be interesting for the reduction of interventions for the patients and for the economic aspect of the healthcare system

Conditions

Timeline

Start date
2019-12-09
Primary completion
2020-01-31
Completion
2020-03-31
First posted
2019-12-16
Last updated
2020-01-10

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT04200014. Inclusion in this directory is not an endorsement.